ichthyosiform การใช้

• Children who survive the neonatal period usually evolve to a less severe phenotype, resembling a severe congenital ichthyosiform erythroderma.
• Ichthyosiform sarcoidosis is a cutaneous condition resembling ichthyosis vulgaris or acquired ichthyosis, with fine scaling usually on the distal extremities, by caused by sarcoidosis.
• Most cases ( approximately 75 % ) of collodion baby will go on to develop a type of autosomal recessive congenital ichthyosis ( either lamellar ichthyosis or congenital ichthyosiform erythrodema ).
• "' Congenital hemidysplasia with ichthyosiform erythroderma and limb defects "'( also known as " CHILD syndrome " ) is a genetic disorder with onset at birth seen almost exclusively in females.
• It is also referred to as "'CHIME syndrome "', after its main symptoms ( colobomas, heart defects, ichthyosiform dermatosis, intellectual disability, and either ear defects or epilepsy ).
• Deletions of " Alox12b " or " Aloxe3 " genes by gene knockout in mice cause a congenital scaly skin disease which is characterized by a greatly reduced skin water barrier function and other features found in the autosomal recessive nonbullous Congenital ichthyosiform erythroderma ( ARCI ) disease of humans .; ARCI refers to nonsyndromic ( i . e . not associated with other signs or symptoms ) congenital Ichthyosis including Harlequin-type ichthyosis, Lamellar ichthyosis, and Congenital ichthyosiform erythroderma.
• Deletions of " Alox12b " or " Aloxe3 " genes by gene knockout in mice cause a congenital scaly skin disease which is characterized by a greatly reduced skin water barrier function and other features found in the autosomal recessive nonbullous Congenital ichthyosiform erythroderma ( ARCI ) disease of humans .; ARCI refers to nonsyndromic ( i . e . not associated with other signs or symptoms ) congenital Ichthyosis including Harlequin-type ichthyosis, Lamellar ichthyosis, and Congenital ichthyosiform erythroderma.